Depo-Medrol

Land: Nieuw-Zeeland

Taal: Engels

Bron: Medsafe (Medicines Safety Authority)

Koop het nu

Productkenmerken Productkenmerken (SPC)
14-04-2000

Werkstoffen:

Methylprednisolone acetate 40 mg/mL

Beschikbaar vanaf:

Pharmacia Limited Company trading as Pharmacia

INN (Algemene Internationale Benaming):

Methylprednisolone acetate 40 mg/mL

Dosering:

40 mg/mL

farmaceutische vorm:

Injection (depot)

Samenstelling:

Active: Methylprednisolone acetate 40 mg/mL

Eenheden in pakket:

Syringe, Pre-filled 1 x 2 mL, 2 mL

klasse:

Prescription

Prescription-type:

Prescription

Geproduceerd door:

Pharmacia & Upjohn Company LLC

Product samenvatting:

Package - Contents - Shelf Life: Syringe, Pre-filled 1 x 2 mL - 2 mL - 60 months from date of manufacture stored at or below 30°C

Autorisatie datum:

1987-12-01

Productkenmerken

                                Version: pfddepmi11123
Supersedes: pfddepmi10323
Page 1 of 25
NEW ZEALAND DATA SHEET
1. PRODUCT NAME
Depo-Medrol
®
40 mg/mL Suspension for Injection
2. QUALITATIVE AND QUANTITATIVE COMPOSITION
Each 1 mL vial contains 40 mg/mL methylprednisolone acetate.
EXCIPIENTS WITH KNOWN EFFECTS:
•
Sodium
•
Macrogol
For the full list of excipients, see section 6.1.
3. PHARMACEUTICAL FORM
Depo-Medrol is a white, aqueous, sterile suspension.
4. CLINICAL PARTICULARS
4.1 THERAPEUTIC INDICATIONS
A. FOR INTRAMUSCULAR ADMINISTRATION
When oral therapy is not feasible and the strength, dosage form, and
route of administration of the
drug reasonably lend the preparation to the treatment of the
condition, the intramuscular use of
Depo-Medrol is indicated as follows:
_ENDOCRINE DISORDERS _
•
Primary or secondary adrenocortical insufficiency (hydrocortisone or
cortisone is the drug of
choice; synthetic analogs may be used in conjunction with
mineralocorticoids where
applicable; in infancy; mineralocorticoid supplementation is of
particular importance).
•
Acute adrenocortical insufficiency (hydrocortisone or cortisone is the
drug of choice;
mineralocorticoid supplementation may be necessary, particularly when
synthetic analogs are
used).
•
Congenital adrenal hyperplasia.
•
Hypercalcaemia associated with cancer.
Version: pfddepmi11123
Supersedes: pfddepmi10323
Page 2 of 25
•
Nonsuppurative thyroiditis.
_RHEUMATIC DISORDERS _
As adjunctive therapy for short-term administration (to tide the
patient over an acute episode or
exacerbation) in:
•
Post-traumatic osteoarthritis
•
Synovitis of osteoarthritis
•
Rheumatoid arthritis, including juvenile rheumatoid arthritis
(selected cases may require
low-dose maintenance therapy)
•
Acute and subacute bursitis
•
Epicondylitis
•
Acute nonspecific tenosynovitis
•
Acute gouty arthritis
•
Psoriatic arthritis
•
Ankylosing spondylitis.
_COLLAGEN DISEASES _
During an exacerbation or as maintenance therapy in selected cases of:
•
Systemic lupus erythematosus
•
Systemic derm
                                
                                Lees het volledige document
                                
                            

Zoekwaarschuwingen met betrekking tot dit product

Bekijk de geschiedenis van documenten